Analysis Of Beer's Law Froot Loops

Finally I put the bung in the volumetric flask, and I relentlessly inverted it to fully mix the solution.

Procedure: In this experiment, various chemicals were mixed together, to determine a reaction. Using two drops from chemical 1 and two drops of chemical two, unless otherwise stated, then recording the type of physical reaction or color changes that occurred.

After added, pick up the beaker and swirl it around lightly for a short period of time.

Discard the solution in the appropriate container as directed to you by your lab instructor.

lab bench. Place a beaker from the drawer on the stir plate. Drag the bottle of NH3 to the 5 mL graduated cylinder (the smallest one) by the sink and fill the cylinder by dropping the bottle on the cylinder. Now drag the 5 mL graduated cylinder to the beaker on the stir plate and add the 5 mL of

Our purpose in this lab was to create four solutions of the same components and different concentration. I found the concentration in Molarity (mol/liter). I would dilute a solution to create new solutions, using the formula M1xV1=M2xV2 where M=molarity and V=volume. In this lab, there were four solutions, Solution A, Solution B, Solution C, and Solution D. The solute or substance that dissolves was sugar and the solvent or substance that the solute dissolves in was water. For Solution A, I weighed 3.42 g sugar and diluted to 100 mL to get a concentration of 0.10 M and the color of bright red. For Solution B, I weighed 0.342 g sugar and diluted to 100 mL to get a concentration of 0.010 M and the color of pink. For Solution C, I measured 10

B.|HCl + BTB|A3|The mixture turned yellow instantly. Under white paper the mixture was more of mustard yellow and under black paper it was less of a bright yellow. |

In the scenario described in problem 7, what is the amount (in moles) of excess

14) Let the crystals of the silver settle in the plastic container and decant off the liquid.

When filling up the burette it is important that a funnel is used, however as the solution reaches the 0 mark it is ideal that the funnel be removed and a pipette used instead to reach the 0 mark, this is to achieve greater precision. During the experiment, it is important to swirl the flask continuously with one hand

2) Rinse the solid with about 30 mL of distilled water and decant the liquid from the solid. It is critical that as little solid as possible is lost during this process. Repeat the rinsing two or three times.

3. A few drops of 6 M acetic acid were added until it became basic.

In order to do this we needed to grab the filter paper with tweezers and hold it above the beaker while using a squeeze bottle to try to get all of the product into the beaker. While doing this the filter paper had dropped into the beaker twice. We had continued to pick it up and try to get most of the mixture off of the filter paper. After we collected the remaining mixture into the beaker we then had to leave for the day, so we placed a paper over the beaker so nothing could contaminate it over night. While cleaning the products we noticed that some of the product was not able to come off the flask beaker, tweezer, glass rod, gloves, squeeze bottle and filter paper. The amount that we had lost had us starting to think that out yield percentage was going to be very low. The following day we had continued to get everything ready to continue the lab, when we were getting the the Buchner Funnel ready, we found out there was a bigger Buchner Funnel and had switched them out. We also got a new filter paper that didn’t needed to be cut. As we placed the Buchner Funnel on to the Filter flask, we then add the filter paper and began to pour the solution into the Buchner

In this experiment, a saturated calcium sulfate was already made and ready to use. 25.00 mL of this solution was then mixed with 10 mL of an ammonia buffer and 1 drop of

I predict that out of the 20 solutions that we are going to be testing, about 6 of them will be an acid, 3 will be neutral and 11 will be a base.